Reaktion #307749

ord-11b37ea7920a4c4686c73b7c6db923d6

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenConcentrate in vacuo

Vorschrift

Dissolve {4-[4-(1,5-dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl-3′-yl]-phenyl}-methanol (1.00 g, 2.64 mmol) in DCM (60 mL). Add thionyl chloride (6 mL) and stir at room temperature for 2 hr. Concentrate in vacuo to give 3′-(4-chloromethyl-phenyl)-4-(1,5-dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl dihydrochloride as a yellow solid (1.20 g, 100%). MS (ES): m/z=397 [M+H]+

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08202873B2uspto-grants-2012_06